Cranbury Medical Labs, Inc.
Mchenry, IL, US
Cranbury Medical Labs, Inc. appears in FDA device records in Mchenry, IL. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Cranbury Medical Labs, Inc. in 1982.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 7 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K828586 | ENTREKIN MODEL DX-300 CONTINUOUS WAVE ULTRASONIC DOPPLER TRANSDUCER | Substantially Equivalent | ||
| K822830 | MEDICAL LABS FETAL SCAN #1000 W/CENTRAL | HGM | Substantially Equivalent | |
| K827718 | UNKNOWN | Substantially Equivalent | ||
| K827376 | BIOPSY GUIDE ATTACHMENT FOR USE WITH FETASCAN 800 | Substantially Equivalent | ||
| K827375 | BIOPSY GUIDE ATTACHMENT FOR USE WITH FETASCAN 2000 AND 2000A | Substantially Equivalent | ||
| K813457 | FETASCAN 2000,2000A OBSTETRICAL DATA | HGM | Substantially Equivalent | |
| K813458 | FETASCAN 1000, 1000A OBSTETRICAL DATA | HGM | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain